FDA Inspection 1278904 — Vincent DiGiovanni, DO

Vincent DiGiovanni, DO — FEI 3038623179

The FDA completed an inspection of Vincent DiGiovanni, DO on August 18, 2025 in Wynnewood, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 18, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Wynnewood, PA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations